In an effort to spread more awareness about lymphedema, and to make sure that all patients know about the new coverage that might be available to them thanks to passage of the Lymphedema Treatment Act, we have stepped up our presence on social media!
If you are on any of these social media networks, please help us get the word out by liking and following us, and also by liking and sharing our posts. The following links will take you straight to our pages:
With a few simple clicks, you can make a difference!
Heather Ferguson
Founder & Executive Director
Lymphedema Advocacy Group
LymphedemaAdvocacyGroup.org
